QA Specialist - 24/7 Shift

Hyper Recruitment Solutions Ltd; Waterford; Presencial; EUR 55.000 - 83.000; Jornada completa

Descripción de la vacante

Hyper Recruitment Solutions Ltd is seeking a Quality Assurance (QA) Specialist for a leading Pharmaceutical company in County Waterford. The role ensures products are manufactured, stored and packaged in line with cGMP.

The position is a 12-month contract with a 24/7 shift pattern: two days (07:00-19:00), two nights (19:00-07:00), followed by four days off. You will support GMP training, document review and audits.

Formación

• Bachelor's degree in a scientific discipline.
• Proven experience in a GMP environment.
• Working knowledge of cGMP regulations.

Responsabilidades

• Support GMP training package development and delivery.
• Prepare and review procedures and batch documentation.
• Conduct audits of all departments according to the plan.

Conocimientos

GMP knowledge

Quality assurance

Audits

Training development

Educación

Bachelor's degree in science

Descripción del empleo

We are recruiting a Quality Assurance (QA) Specialist to join a leading Pharmaceutical company in the County Waterford area. As the Quality Assurance (QA) Specialist, you will play a crucial role in ensuring that products are manufactured, stored, and packaged in accordance with current Good Manufacturing Practices (cGMP).

This is an initial 12 month contract with likely extension. Please note this is on a 24/7 shift pattern - Two days (07:00-19:00), two nights (19:00-07:00), followed by four days off.

Key Duties And Responsibilities

• As the Quality Assurance (QA) Specialist, you will work as part of the Quality Assurance team to ensure compliance with cGMP.
• As the Quality Assurance (QA) Specialist, you will support the development and delivery of GMP training packages.
• As the Quality Assurance (QA) Specialist, you will participate in the preparation and review of procedures and batch documentation.
• As the Quality Assurance (QA) Specialist, you will conduct audits of all departments according to the agreed schedule.

Role Requirements

• Relevant degree in a scientific or related discipline.
• Proven industry experience in a similar role within a GMP environment.
• A working knowledge and practical experience with cGMP regulations.

Key Words: Quality Assurance / GMP / cGMP / Pharmaceutical / Batch Documentation / Audits / Quality Systems / Continuous Improvement / Regulatory Compliance / Training Packages / Quality Specialist

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.